Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16969968 | 0.653 | 0.360 | 15 | 78590583 | missense variant | G/A | snv | 0.26 | 0.24 | 4 | |
rs2629540 | 0.925 | 0.080 | 10 | 124737579 | intron variant | G/C | snv | 0.18 | 3 | ||
rs684513 | 0.925 | 0.080 | 15 | 78566058 | intron variant | C/G;T | snv | 3 | |||
rs111325002 | 1.000 | 0.080 | 3 | 96134788 | intergenic variant | A/G | snv | 8.6E-03 | 2 | ||
rs150954431 | 1.000 | 0.080 | 12 | 124517777 | intron variant | C/T | snv | 1.6E-02 | 2 | ||
rs2005290 | 1.000 | 0.080 | 17 | 3284718 | intron variant | C/G;T | snv | 2 | |||
rs12071360 | 1.000 | 0.080 | 1 | 233608833 | intergenic variant | T/C | snv | 0.10 | 1 | ||
rs13273442 | 0.882 | 0.080 | 8 | 42688874 | intergenic variant | A/G | snv | 0.66 | 1 |